FDA Warning Letter — Mark Berman, M.D.

Case 562321 — FEI 3010907482

The FDA took a Warning Letter action against Mark Berman, M.D. on Feb 13, 2019 (Beverly Hills, CA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Mark Berman, M.D.
Date
Feb 13, 2019
Fiscal Year
2019
Product Type
Devices
Center
CDRH
Location
Beverly Hills, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.